Canonical Allele Identifier: CA2634948255

Gene: ANKRD11

Linked Data

• gnomAD v4: 16-89285249-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89285252_89285253del , CM000678.2:g.89285252_89285253del	GRCh38
NC_000016.9:g.89351660_89351661del , CM000678.1:g.89351660_89351661del	GRCh37
NC_000016.8:g.87879161_87879162del	NCBI36
NG_032003.1:g.210311_210312del
NG_032003.2:g.210311_210312del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.1291_1292del MANE Select	ENSP00000301030.4:p.His431TyrfsTer6
ENST00000330736.10:c.*1094_*1095del	ENSP00000330815.5:n.*1094_*1095del
ENST00000378330.7:c.1291_1292del	ENSP00000367581.2:p.His431TyrfsTer6
ENST00000568100.2:n.997_998del
ENST00000642443.1:c.916_917del	ENSP00000493644.1:p.His306TyrfsTer6
ENST00000642600.1:c.1291_1292del	ENSP00000495226.1:p.His431TyrfsTer6
ENST00000644285.1:c.744+3277_744+3278del	ENSP00000496476.1:n.744+3277_744+3278del
ENST00000645212.1:n.3063_3064del
ENST00000646345.1:n.1283_1284del
ENST00000301030.8:c.1291_1292del	ENSP00000301030.4:p.His431TyrfsTer6
ENST00000330736.9:c.*1094_*1095del	ENSP00000330815.5:n.*1094_*1095del
ENST00000378330.6:c.1291_1292del	ENSP00000367581.2:p.His431TyrfsTer6
ENST00000562194.1:c.151+3277_151+3278del
ENST00000568100.1:n.842_843del
ENST00000613312.4:c.*189_*190del	ENSP00000478018.1:n.*189_*190del
NM_001256182.1:c.1291_1292del	NP_001243111.1:p.His431TyrfsTer6
NM_001256183.1:c.1291_1292del	NP_001243112.1:p.His431TyrfsTer6
NM_013275.5:c.1291_1292del	NP_037407.4:p.His431TyrfsTer6
XM_006721181.1:c.1189_1190del	XP_006721244.1:p.His397TyrfsTer6
XM_006721184.2:c.994_995del	XP_006721247.1:p.His332TyrfsTer6
XM_011523051.1:c.1291_1292del	XP_011521353.1:p.His431TyrfsTer6
XM_011523052.1:c.1291_1292del	XP_011521354.1:p.His431TyrfsTer6
XM_011523053.1:c.1291_1292del	XP_011521355.1:p.His431TyrfsTer6
XM_011523054.1:c.1189_1190del	XP_011521356.1:p.His397TyrfsTer6
XM_011523055.1:c.1189_1190del	XP_011521357.1:p.His397TyrfsTer6
XM_011523056.1:c.1162_1163del	XP_011521358.1:p.His388TyrfsTer6
XM_011523057.1:c.1291_1292del	XP_011521359.1:p.His431TyrfsTer6
XM_011523051.3:c.1291_1292del	XP_011521353.1:p.His431TyrfsTer6
XM_011523053.2:c.1291_1292del	XP_011521355.1:p.His431TyrfsTer6
XM_011523054.2:c.1189_1190del	XP_011521356.1:p.His397TyrfsTer6
XM_011523055.2:c.1189_1190del	XP_011521357.1:p.His397TyrfsTer6
XM_011523056.2:c.1162_1163del	XP_011521358.1:p.His388TyrfsTer6
XM_011523057.2:c.1291_1292del	XP_011521359.1:p.His431TyrfsTer6
XM_017023182.2:c.1291_1292del	XP_016878671.1:p.His431TyrfsTer6
XM_017023183.1:c.1291_1292del	XP_016878672.1:p.His431TyrfsTer6
XM_017023184.1:c.1291_1292del	XP_016878673.1:p.His431TyrfsTer6
XM_017023185.1:c.1291_1292del	XP_016878674.1:p.His431TyrfsTer6
XM_017023186.1:c.1291_1292del	XP_016878675.1:p.His431TyrfsTer6
XM_017023187.1:c.1291_1292del	XP_016878676.1:p.His431TyrfsTer6
XM_024450244.1:c.1189_1190del	XP_024306012.1:p.His397TyrfsTer6
NM_013275.6:c.1291_1292del MANE Select	NP_037407.4:p.His431TyrfsTer6
NM_001256182.2:c.1291_1292del	NP_001243111.1:p.His431TyrfsTer6
NM_001256183.2:c.1291_1292del	NP_001243112.1:p.His431TyrfsTer6